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Effect of miR-1 loss on metabolic flexibility and exercise performance. (A) Respiratory exchange ratio (RER) via indirect calorimetry over a 48-hr period. (B) Box plots (min-to-max) showing median and interquartile range (IQR) for RER data. (C) Whole-body oxygen consumption (VO2) and (D) locomotor activity during indirect calorimetry period. Data in A-D are mean ± SEM, plotted using CalR (Ver. 2), and analyzed using a two-way ANOVA for light and dark cycles separately. (E) Fasting basal blood glucose levels, data analyzed using independent t -tests (2-tailed). (F) Glucose tolerance test (GTT), data are mean ± SD, data analyzed by two-way ANOVA, main effect of miR-1 knockout (KO) and interaction (genotype x time) shown. Data in A-F from n = 5 female wild-type (WT) mice and n = 5 female miR-1 KO mice. (G – H) <t>ClockLab</t> analyses of 4 weeks of voluntary wheel running. Average (G) daily running volume (km/day) and (H) maximum running bout (sec). Data in G-H from n = 5 female mice per group. (I – J) CeLeST analysis of (I) wave initiation rate and (J) activity index in Untrained N2 (WT) (n = 32) and mir-1 mutant worms (n = 35). (K – L) CeLeST analysis of (K) wave initiation rate and (L) activity index in Untrained (dark circle) or Exercised (open circle) N2 (n = 32 and n = 36, respectively), and Untrained (dark square) and Exercised (open square) mir-1 mutant worms (n = 35 and n = 36, respectively). Data in I-J analyzed using independent t -tests (2-tailed). Data in K-L analyzed using a two-way ANOVA, main effect of miR-1 KO, interaction (genotype x exercise), and results of post-hoc Tukey's multiple comparisons tests shown. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗∗ p < 0.0001, ns: not significant.
Clocklab Software, supplied by Actimetrics Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Effect of miR-1 loss on metabolic flexibility and exercise performance. (A) Respiratory exchange ratio (RER) via indirect calorimetry over a 48-hr period. (B) Box plots (min-to-max) showing median and interquartile range (IQR) for RER data. (C) Whole-body oxygen consumption (VO2) and (D) locomotor activity during indirect calorimetry period. Data in A-D are mean ± SEM, plotted using CalR (Ver. 2), and analyzed using a two-way ANOVA for light and dark cycles separately. (E) Fasting basal blood glucose levels, data analyzed using independent t -tests (2-tailed). (F) Glucose tolerance test (GTT), data are mean ± SD, data analyzed by two-way ANOVA, main effect of miR-1 knockout (KO) and interaction (genotype x time) shown. Data in A-F from n = 5 female wild-type (WT) mice and n = 5 female miR-1 KO mice. (G – H) <t>ClockLab</t> analyses of 4 weeks of voluntary wheel running. Average (G) daily running volume (km/day) and (H) maximum running bout (sec). Data in G-H from n = 5 female mice per group. (I – J) CeLeST analysis of (I) wave initiation rate and (J) activity index in Untrained N2 (WT) (n = 32) and mir-1 mutant worms (n = 35). (K – L) CeLeST analysis of (K) wave initiation rate and (L) activity index in Untrained (dark circle) or Exercised (open circle) N2 (n = 32 and n = 36, respectively), and Untrained (dark square) and Exercised (open square) mir-1 mutant worms (n = 35 and n = 36, respectively). Data in I-J analyzed using independent t -tests (2-tailed). Data in K-L analyzed using a two-way ANOVA, main effect of miR-1 KO, interaction (genotype x exercise), and results of post-hoc Tukey's multiple comparisons tests shown. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗∗ p < 0.0001, ns: not significant.
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Effect of miR-1 loss on metabolic flexibility and exercise performance. (A) Respiratory exchange ratio (RER) via indirect calorimetry over a 48-hr period. (B) Box plots (min-to-max) showing median and interquartile range (IQR) for RER data. (C) Whole-body oxygen consumption (VO2) and (D) locomotor activity during indirect calorimetry period. Data in A-D are mean ± SEM, plotted using CalR (Ver. 2), and analyzed using a two-way ANOVA for light and dark cycles separately. (E) Fasting basal blood glucose levels, data analyzed using independent t -tests (2-tailed). (F) Glucose tolerance test (GTT), data are mean ± SD, data analyzed by two-way ANOVA, main effect of miR-1 knockout (KO) and interaction (genotype x time) shown. Data in A-F from n = 5 female wild-type (WT) mice and n = 5 female miR-1 KO mice. (G – H) <t>ClockLab</t> analyses of 4 weeks of voluntary wheel running. Average (G) daily running volume (km/day) and (H) maximum running bout (sec). Data in G-H from n = 5 female mice per group. (I – J) CeLeST analysis of (I) wave initiation rate and (J) activity index in Untrained N2 (WT) (n = 32) and mir-1 mutant worms (n = 35). (K – L) CeLeST analysis of (K) wave initiation rate and (L) activity index in Untrained (dark circle) or Exercised (open circle) N2 (n = 32 and n = 36, respectively), and Untrained (dark square) and Exercised (open square) mir-1 mutant worms (n = 35 and n = 36, respectively). Data in I-J analyzed using independent t -tests (2-tailed). Data in K-L analyzed using a two-way ANOVA, main effect of miR-1 KO, interaction (genotype x exercise), and results of post-hoc Tukey's multiple comparisons tests shown. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗∗ p < 0.0001, ns: not significant.
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Effect of miR-1 loss on metabolic flexibility and exercise performance. (A) Respiratory exchange ratio (RER) via indirect calorimetry over a 48-hr period. (B) Box plots (min-to-max) showing median and interquartile range (IQR) for RER data. (C) Whole-body oxygen consumption (VO2) and (D) locomotor activity during indirect calorimetry period. Data in A-D are mean ± SEM, plotted using CalR (Ver. 2), and analyzed using a two-way ANOVA for light and dark cycles separately. (E) Fasting basal blood glucose levels, data analyzed using independent t -tests (2-tailed). (F) Glucose tolerance test (GTT), data are mean ± SD, data analyzed by two-way ANOVA, main effect of miR-1 knockout (KO) and interaction (genotype x time) shown. Data in A-F from n = 5 female wild-type (WT) mice and n = 5 female miR-1 KO mice. (G – H) <t>ClockLab</t> analyses of 4 weeks of voluntary wheel running. Average (G) daily running volume (km/day) and (H) maximum running bout (sec). Data in G-H from n = 5 female mice per group. (I – J) CeLeST analysis of (I) wave initiation rate and (J) activity index in Untrained N2 (WT) (n = 32) and mir-1 mutant worms (n = 35). (K – L) CeLeST analysis of (K) wave initiation rate and (L) activity index in Untrained (dark circle) or Exercised (open circle) N2 (n = 32 and n = 36, respectively), and Untrained (dark square) and Exercised (open square) mir-1 mutant worms (n = 35 and n = 36, respectively). Data in I-J analyzed using independent t -tests (2-tailed). Data in K-L analyzed using a two-way ANOVA, main effect of miR-1 KO, interaction (genotype x exercise), and results of post-hoc Tukey's multiple comparisons tests shown. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗∗ p < 0.0001, ns: not significant.
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Effect of miR-1 loss on metabolic flexibility and exercise performance. (A) Respiratory exchange ratio (RER) via indirect calorimetry over a 48-hr period. (B) Box plots (min-to-max) showing median and interquartile range (IQR) for RER data. (C) Whole-body oxygen consumption (VO2) and (D) locomotor activity during indirect calorimetry period. Data in A-D are mean ± SEM, plotted using CalR (Ver. 2), and analyzed using a two-way ANOVA for light and dark cycles separately. (E) Fasting basal blood glucose levels, data analyzed using independent t -tests (2-tailed). (F) Glucose tolerance test (GTT), data are mean ± SD, data analyzed by two-way ANOVA, main effect of miR-1 knockout (KO) and interaction (genotype x time) shown. Data in A-F from n = 5 female wild-type (WT) mice and n = 5 female miR-1 KO mice. (G – H) <t>ClockLab</t> analyses of 4 weeks of voluntary wheel running. Average (G) daily running volume (km/day) and (H) maximum running bout (sec). Data in G-H from n = 5 female mice per group. (I – J) CeLeST analysis of (I) wave initiation rate and (J) activity index in Untrained N2 (WT) (n = 32) and mir-1 mutant worms (n = 35). (K – L) CeLeST analysis of (K) wave initiation rate and (L) activity index in Untrained (dark circle) or Exercised (open circle) N2 (n = 32 and n = 36, respectively), and Untrained (dark square) and Exercised (open square) mir-1 mutant worms (n = 35 and n = 36, respectively). Data in I-J analyzed using independent t -tests (2-tailed). Data in K-L analyzed using a two-way ANOVA, main effect of miR-1 KO, interaction (genotype x exercise), and results of post-hoc Tukey's multiple comparisons tests shown. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗∗ p < 0.0001, ns: not significant.
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Effect of miR-1 loss on metabolic flexibility and exercise performance. (A) Respiratory exchange ratio (RER) via indirect calorimetry over a 48-hr period. (B) Box plots (min-to-max) showing median and interquartile range (IQR) for RER data. (C) Whole-body oxygen consumption (VO2) and (D) locomotor activity during indirect calorimetry period. Data in A-D are mean ± SEM, plotted using CalR (Ver. 2), and analyzed using a two-way ANOVA for light and dark cycles separately. (E) Fasting basal blood glucose levels, data analyzed using independent t -tests (2-tailed). (F) Glucose tolerance test (GTT), data are mean ± SD, data analyzed by two-way ANOVA, main effect of miR-1 knockout (KO) and interaction (genotype x time) shown. Data in A-F from n = 5 female wild-type (WT) mice and n = 5 female miR-1 KO mice. (G – H) <t>ClockLab</t> analyses of 4 weeks of voluntary wheel running. Average (G) daily running volume (km/day) and (H) maximum running bout (sec). Data in G-H from n = 5 female mice per group. (I – J) CeLeST analysis of (I) wave initiation rate and (J) activity index in Untrained N2 (WT) (n = 32) and mir-1 mutant worms (n = 35). (K – L) CeLeST analysis of (K) wave initiation rate and (L) activity index in Untrained (dark circle) or Exercised (open circle) N2 (n = 32 and n = 36, respectively), and Untrained (dark square) and Exercised (open square) mir-1 mutant worms (n = 35 and n = 36, respectively). Data in I-J analyzed using independent t -tests (2-tailed). Data in K-L analyzed using a two-way ANOVA, main effect of miR-1 KO, interaction (genotype x exercise), and results of post-hoc Tukey's multiple comparisons tests shown. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗∗ p < 0.0001, ns: not significant.
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Effect of miR-1 loss on metabolic flexibility and exercise performance. (A) Respiratory exchange ratio (RER) via indirect calorimetry over a 48-hr period. (B) Box plots (min-to-max) showing median and interquartile range (IQR) for RER data. (C) Whole-body oxygen consumption (VO2) and (D) locomotor activity during indirect calorimetry period. Data in A-D are mean ± SEM, plotted using CalR (Ver. 2), and analyzed using a two-way ANOVA for light and dark cycles separately. (E) Fasting basal blood glucose levels, data analyzed using independent t -tests (2-tailed). (F) Glucose tolerance test (GTT), data are mean ± SD, data analyzed by two-way ANOVA, main effect of miR-1 knockout (KO) and interaction (genotype x time) shown. Data in A-F from n = 5 female wild-type (WT) mice and n = 5 female miR-1 KO mice. (G – H) <t>ClockLab</t> analyses of 4 weeks of voluntary wheel running. Average (G) daily running volume (km/day) and (H) maximum running bout (sec). Data in G-H from n = 5 female mice per group. (I – J) CeLeST analysis of (I) wave initiation rate and (J) activity index in Untrained N2 (WT) (n = 32) and mir-1 mutant worms (n = 35). (K – L) CeLeST analysis of (K) wave initiation rate and (L) activity index in Untrained (dark circle) or Exercised (open circle) N2 (n = 32 and n = 36, respectively), and Untrained (dark square) and Exercised (open square) mir-1 mutant worms (n = 35 and n = 36, respectively). Data in I-J analyzed using independent t -tests (2-tailed). Data in K-L analyzed using a two-way ANOVA, main effect of miR-1 KO, interaction (genotype x exercise), and results of post-hoc Tukey's multiple comparisons tests shown. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗∗ p < 0.0001, ns: not significant.
Lomb Scargle Periodogram Analysis Clocklab 6.1.15, supplied by Actimetrics Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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clocklab  (Actimetrics Inc)
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Effect of miR-1 loss on metabolic flexibility and exercise performance. (A) Respiratory exchange ratio (RER) via indirect calorimetry over a 48-hr period. (B) Box plots (min-to-max) showing median and interquartile range (IQR) for RER data. (C) Whole-body oxygen consumption (VO2) and (D) locomotor activity during indirect calorimetry period. Data in A-D are mean ± SEM, plotted using CalR (Ver. 2), and analyzed using a two-way ANOVA for light and dark cycles separately. (E) Fasting basal blood glucose levels, data analyzed using independent t -tests (2-tailed). (F) Glucose tolerance test (GTT), data are mean ± SD, data analyzed by two-way ANOVA, main effect of miR-1 knockout (KO) and interaction (genotype x time) shown. Data in A-F from n = 5 female wild-type (WT) mice and n = 5 female miR-1 KO mice. (G – H) <t>ClockLab</t> analyses of 4 weeks of voluntary wheel running. Average (G) daily running volume (km/day) and (H) maximum running bout (sec). Data in G-H from n = 5 female mice per group. (I – J) CeLeST analysis of (I) wave initiation rate and (J) activity index in Untrained N2 (WT) (n = 32) and mir-1 mutant worms (n = 35). (K – L) CeLeST analysis of (K) wave initiation rate and (L) activity index in Untrained (dark circle) or Exercised (open circle) N2 (n = 32 and n = 36, respectively), and Untrained (dark square) and Exercised (open square) mir-1 mutant worms (n = 35 and n = 36, respectively). Data in I-J analyzed using independent t -tests (2-tailed). Data in K-L analyzed using a two-way ANOVA, main effect of miR-1 KO, interaction (genotype x exercise), and results of post-hoc Tukey's multiple comparisons tests shown. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗∗ p < 0.0001, ns: not significant.
Clocklab, supplied by Actimetrics Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Effect of miR-1 loss on metabolic flexibility and exercise performance. (A) Respiratory exchange ratio (RER) via indirect calorimetry over a 48-hr period. (B) Box plots (min-to-max) showing median and interquartile range (IQR) for RER data. (C) Whole-body oxygen consumption (VO2) and (D) locomotor activity during indirect calorimetry period. Data in A-D are mean ± SEM, plotted using CalR (Ver. 2), and analyzed using a two-way ANOVA for light and dark cycles separately. (E) Fasting basal blood glucose levels, data analyzed using independent t -tests (2-tailed). (F) Glucose tolerance test (GTT), data are mean ± SD, data analyzed by two-way ANOVA, main effect of miR-1 knockout (KO) and interaction (genotype x time) shown. Data in A-F from n = 5 female wild-type (WT) mice and n = 5 female miR-1 KO mice. (G – H) ClockLab analyses of 4 weeks of voluntary wheel running. Average (G) daily running volume (km/day) and (H) maximum running bout (sec). Data in G-H from n = 5 female mice per group. (I – J) CeLeST analysis of (I) wave initiation rate and (J) activity index in Untrained N2 (WT) (n = 32) and mir-1 mutant worms (n = 35). (K – L) CeLeST analysis of (K) wave initiation rate and (L) activity index in Untrained (dark circle) or Exercised (open circle) N2 (n = 32 and n = 36, respectively), and Untrained (dark square) and Exercised (open square) mir-1 mutant worms (n = 35 and n = 36, respectively). Data in I-J analyzed using independent t -tests (2-tailed). Data in K-L analyzed using a two-way ANOVA, main effect of miR-1 KO, interaction (genotype x exercise), and results of post-hoc Tukey's multiple comparisons tests shown. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗∗ p < 0.0001, ns: not significant.

Journal: Molecular Metabolism

Article Title: microRNA-1 regulates metabolic flexibility by programming adult skeletal muscle pyruvate metabolism

doi: 10.1016/j.molmet.2025.102182

Figure Lengend Snippet: Effect of miR-1 loss on metabolic flexibility and exercise performance. (A) Respiratory exchange ratio (RER) via indirect calorimetry over a 48-hr period. (B) Box plots (min-to-max) showing median and interquartile range (IQR) for RER data. (C) Whole-body oxygen consumption (VO2) and (D) locomotor activity during indirect calorimetry period. Data in A-D are mean ± SEM, plotted using CalR (Ver. 2), and analyzed using a two-way ANOVA for light and dark cycles separately. (E) Fasting basal blood glucose levels, data analyzed using independent t -tests (2-tailed). (F) Glucose tolerance test (GTT), data are mean ± SD, data analyzed by two-way ANOVA, main effect of miR-1 knockout (KO) and interaction (genotype x time) shown. Data in A-F from n = 5 female wild-type (WT) mice and n = 5 female miR-1 KO mice. (G – H) ClockLab analyses of 4 weeks of voluntary wheel running. Average (G) daily running volume (km/day) and (H) maximum running bout (sec). Data in G-H from n = 5 female mice per group. (I – J) CeLeST analysis of (I) wave initiation rate and (J) activity index in Untrained N2 (WT) (n = 32) and mir-1 mutant worms (n = 35). (K – L) CeLeST analysis of (K) wave initiation rate and (L) activity index in Untrained (dark circle) or Exercised (open circle) N2 (n = 32 and n = 36, respectively), and Untrained (dark square) and Exercised (open square) mir-1 mutant worms (n = 35 and n = 36, respectively). Data in I-J analyzed using independent t -tests (2-tailed). Data in K-L analyzed using a two-way ANOVA, main effect of miR-1 KO, interaction (genotype x exercise), and results of post-hoc Tukey's multiple comparisons tests shown. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗∗ p < 0.0001, ns: not significant.

Article Snippet: A wireless node was used to sense wheel revolutions from the rotation of a magnet mounted on the wheel axle, recorded via the ClockLab software (Actimetrics).

Techniques: Activity Assay, Knock-Out, Mutagenesis